Canonical Allele Identifier: CA369861556

Gene: KCNH2

Linked Data

• dbSNP Id: rs1801408103
• gnomAD v3: 7-150957359-T-C
• gnomAD v4: 7-150957359-T-C
• MyVariant Identifiers: chr7:g.150654447T>C (hg19) ; chr7:g.150957359T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957359T>C , CM000669.2:g.150957359T>C	GRCh38
NC_000007.13:g.150654447T>C , CM000669.1:g.150654447T>C	GRCh37
NC_000007.12:g.150285380T>C	NCBI36
NG_008916.1:g.25568A>G , LRG_288:g.25568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1893A>G
ENST00000262186.10:c.1060A>G MANE Select	ENSP00000262186.5:p.Ser354Gly
ENST00000262186.9:c.1060A>G	ENSP00000262186.5:p.Ser354Gly
ENST00000430723.4:c.712A>G	ENSP00000387657.4:p.Ser238Gly
ENST00000532957.5:n.1283A>G
NM_000238.3:c.1060A>G , LRG_288t1:c.1060A>G	NP_000229.1:p.Ser354Gly
NM_172056.2:c.1060A>G , LRG_288t2:c.1060A>G	NP_742053.1:p.Ser354Gly
XM_011516185.1:c.760A>G	XP_011514487.1:p.Ser254Gly
XM_011516186.1:c.1060A>G	XP_011514488.1:p.Ser354Gly
XM_011516185.2:c.760A>G	XP_011514487.1:p.Ser254Gly
XM_011516186.3:c.1060A>G	XP_011514488.1:p.Ser354Gly
XM_017012195.1:c.910A>G	XP_016867684.1:p.Ser304Gly
XM_017012196.1:c.883A>G	XP_016867685.1:p.Ser295Gly
NM_000238.4:c.1060A>G MANE Select	NP_000229.1:p.Ser354Gly